Manager, Clinical Risk and Analytics

In this pivotal role, you'll be at the forefront of implementing Risk-Based Quality Management (RBQM) strategies across our studies - from study design through to closeout. Each RBQM Lead is empowered to manage their program across all trial phases, supported by a highly skilled team of analysts and programmers. If you're ready to make a real impact in a collaborative, forward-thinking environment where data meets purpose, we'd love to hear from you. Conduct and manage Study Risk Assessment at start and periodically Develop the centralized monitoring plan Review centralized monitoring study set up for study team. Review findings from CM and review with study team for action Follow up on actions, and guide teams on systemic risks Working at Alnylam: https://www.alnylam.com/careers/working-at-alnylam You'll bring a strong foundation in clinical research in the pharmaceutical or CRO industry. With a degree (or equivalent) in a scientific, analytical, or technical discipline, you have a solid understanding of clinical development processes and are confident in the concepts of study design, conduct, and closeout. Your expertise in clinical trial risk management--paired with your familiarity with centralized monitoring and RBQM principles--positions you to contribute meaningfully from day one. Equally important is your ability to work collaboratively within a dynamic team, managing shifting priorities while maintaining focus on shared goals. You communicate clearly and effectively in English, both in writing and verbally, and are comfortable navigating complex information to deliver high-quality insights and outcomes. If you're a proactive problem-solver who thrives in a fast-paced, science-driven environment, you could be the ideal fit for our team. You will have Strong critical thinking and analytical skills, and Aptitude for data analytics Good understanding and knowledge of risk management concepts and principles Excellent project management capabilities Experience and good understanding of clinical trial data from various sources (e.g. Clinical devices, SDTM, RAVE, IRT, etc.) Knowledge of Good Clinical Practice/ICH E6 (R3), ICH E8 R1 Guidelines and/or other applicable regulatory requirements High degree of accuracy and attention to detail Are you ready to be part of what's next? Join us and help bring groundbreaking RNAi therapies to patients around the world. Next Steps This vacancy will be advertised from Monday, 26th May with a scheduled closing date of Friday, 30th May - we welcome your application as soon as possible.